A- Draw each of the following compounds. 1. 1-Ethoxy-2-bromopropane 2. 3-Ethyl-4-methylcyclohexanethiol 3. 2-Chloro-6-methylthiophenol 4. 4-Chloro-2-methylanisole 5. 1,1,1,4,4,4-Hexafluoro-2,3-di(methylation)2-butene
Q: 1. O3 g. 2. DMS for h. Na NH3 1. mCPBA 1. 2. H30* j. Cl2
A: Organic reaction mechanisms:
Q: SCH3 OCH3 Br N(CH3)2 1 2 3 A) 3>1> 2>4 B) 3> 2>1>4 C) 4 > 2 > 3 >1 D) 1>3> 2 > 4
A: Order the carboxylic acid derivatives from most reactive to least reactive towards nucleophilic…
Q: Supply the missing compounds in the following synthesis scheme. 1. NaNH2 (3 equiv) H CCI4 Br2 1.…
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Q: What is a multi-step synthesis with intermediate steps to produce the following molecule?
A: Multi-step synthesis of this molecule:The IUPAC name is 4, 5 dichloro 6, 6 dimethyl octane. The…
Q: B. In each of the following pairs, circle the species that is more reactive toward nucleophilic…
A: We know that greater electrophilicity of the carbonyl, then faster will be the nucleophilic attack
Q: Br
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Q: Reaction of 1-methoxy-2- methylpropane and HI, heat. Draw the organic product or products formed…
A: Reaction will definitely occur and it will be an SN2 reaction ( I- is nucleophilie ). There are 2…
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A: When terminal alkyne (alkyne that ends with C-H bond) react strong base ....a acid base reaction…
Q: Draw the products of each nucleophilic substitution reaction. d. + CH;CH2OH а. CH3 Br + NaCN +…
A: Note: Since you have posted a question with multiple subparts, we will solve the first three…
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Q: Follow the curved arrows and draw the products of the following reaction.
A: The reactants are protonated form of cyclohexanone and a ethane-1,2-diol . This acid catalysed…
Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…
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Q: + en
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Q: Please identify major PRODUCT A and major PRODUCT B.
A: We have given the organic reaction and we have to identify major PRODUCT A and major PRODUCT B
Q: c) エ
A: c) The conversion of ethynylbenzene to 2-phenylacetaldehyde. Reagent used: Dilute H2SO4/HgSO4. This…
Q: H3CO. 1. NaOCH3 2. H20 OCH3
A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2,-OH and…
Q: CN NaOH HO H20 NC
A: Solution : NaOH and water used as a reagent.NaOH is a base that is used to abstract…
Q: See attached file ?
A: Given:
Q: Draw a stepwise, detailed mechanism for the following reaction. Use curved arrows to show the…
A: Br acts as leaving group and CH3CH2OH as nucleophile, which results into formation of nucleophilic…
Q: Draw the appropriate reagents/ solvent
A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…
Q: COULD EXPLAIN THE FOLLOWING STEPS BY ARROWS IN BASIC SOLUTION CH3 CH3 но CH2CH3 H20 CH2CH3
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Q: CH3-C-CH CHz-
A: This transformation completed in two steps, In first step acyl chloride formation and in next step…
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Q: Draw out the complete mechanism of the reaction and include all relevant electrons and arrows…
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Q: Draw the major product of this reaction. Ignore inorganic byproducts. H3O*
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Q: CO₂E1 i CH3CHCO₂E 1. Na* "Ot 2. PhBr 3. H30, heat The intended reaction is the because the alkyl…
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Q: Label the electrophilic and nucleophilic sites in each molecule.
A: A nucleophile is defined as an electron rich species. It is also known as "nucleus loving" or…
Q: Which of the following could act as a nucleophile?
A: Given:To give which of the following could act as a nucleophile
Q: Draw the product of cyclohex-2-en-1-one and hydrogen cyanide, base catalyzed.
A: The reactants given are cyclohex-2-en-1-one and hydrogen cyanide in base.
Q: Draw a stepwise mechanism for the attached reaction sequence.
A: The given reaction is a good method for alpha alkylation. Here, NaH (sodium hydride) is used as a…
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Q: Match each reaction to a product. Answers may be repeated. Assume any necessary workup. Chiral…
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A: "Since you have posted a question with multiple subparts, we will solve first three sub parts for…
Q: appropriate torg. 5. Aromatic ketones can be prepared by of an aromatic ring 6. Acetaldehyde…
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Q: a. Strong bases are [ Select ] nucleophiles. b. Electron-withdrawing groups nearby a nucleophilic…
A: Bases try to abstract hydrogen whereas nucleophiles attack electron deficit carbon atoms. The groups…
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A: The major products for the given reactions are attached below.
Q: accomplish
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Q: Draw the major organic product or products for the reaction. Multiple products may be drawn in one…
A: The -CF3 group attached to the benzene ring exhibits -I(Inductive effect) due to which it…
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Q: NaOH N2OCH3 H3CO OCH heat
A: "Since you have asked multiple questions, we will solve the first question for you. If you want any…
Q: Which statement best explains why alkylation of an α-carbon works best if the alkyl halide used is a…
A: Formation of carbon-carbon bond through alkylation of alkyl halides occurs via SN2 mechanism. It…
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Q: Choose the two major products of the following reaction.
A: The given reactant i.e. 2-bromopentane is a secondary alkyl halide and the reaction is carried out…
Q: Complete the curved-arrow mechanism for the scheme below by adding any missing atoms, bonds,…
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Q: A)
A: Here we have to prepare the following given compounds from alkyl halide containing four carbon atom…
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A: Addition of excess acid halide to an alkyne would produce a/an ___ dihalide .. answer is given…
Q: Draw the major product of this reaction. Ignore inorganic byproducts. CI excess CH3NH2
A: Here one acid chloride reacts with methylamine. The reaction is between cyclopentanecarbonyl…
Q: Complete the following reactions with the missing reagent(s) or major product(s).
A: Solution: We can see this is the step down reaction in which given molecule is break down into two…
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- design synthesis, show intermediates and reagentsPlease answer this Can you give examples to explain Addition reactions-general characteristics Benzene rings do not reactthi like alkenes Remember, the electrophile adds to the less substituted carbon, and the nucleophile to the more substituted carbon. Markovnikov’s Rule: The addition of a hydrogen halide to an alkene favors the product in which the proton adds to the alkene carbon that is initially bonded to the greater number of hydrogen atoms. Carbocation rearrangements- Methyl groups and hydride groups can migrate to make a more stable carbocation. A primary carbocation is less stable than a secondary carbocation, which is less stable than a tertiary carbocation. Addition of A Strong Bronsted Acid Hydrohalogenation HX addition to an alkene. Goes through a carbocation intermediate. The electrophile (H+) adds to the less substituted carbon, and the carbocation forms on the more substituted carbon. The nucleophile (X-) then adds to the more substituted carbocation.…For the given structure below, what type of TAG is given above? and how many kinds of products will be formed from the saponification of this TAG?